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Nature Genetics|July 4, 2017
The methyltransferase SETDB1 regulates a large neuron-specific topological chromatin domainYan Jiang, Yong-Hwee Eddie Loh, Prashanth Rajarajan, et al.
Journal of the American College of Cardiology|June 30, 2007
Severe myocardial fibrosis caused by a deletion of the 5' end of the lamin A/C geneJ Peter van Tintelen, Rene A Tio, Wilhelmina S Kerstjens-Frederikse, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Desmoglein-2 and desmocollin-2 mutations in dutch arrhythmogenic right ventricular dysplasia/cardiomypathy patients: results from a multicenter studyZahurul A Bhuiyan, Jan D H Jongbloed, Jasper van der Smagt, et al.
Circulation. Genomic and Precision Medicine|February 10, 2021
Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical FeaturesAlice Ghidoni, Perry M Elliott, Petros Syrris, et al.
European Journal of Heart Failure|November 5, 2016
Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathyJoeri A Jansweijer, Karin Nieuwhof, Francesco Russo, et al.
Frontiers in Cardiovascular Medicine|October 14, 2024
Best practices in robotic magnetic navigation-guided catheter ablation of cardiac arrhythmias, a position paper of the Society for Cardiac Robotic NavigationAnna M E Noten, Tamas Szili-Torok, Sabine Ernst, et al.
The American Journal of Cardiology|July 23, 2013
Arrhythmogenic right ventricular dysplasia/cardiomyopathy according to revised 2010 task force criteria with inclusion of non-desmosomal phospholamban mutation carriersJudith A Groeneweg, Paul A van der Zwaag, Louise R A Olde Nordkamp, et al.
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